Szabó G, Nunley K R, Hoffman P L
Department of Pharmacology, University of Colorado Health Sciences Center, Denver 80262, USA.
Eur J Pharmacol. 1996 Jun 13;306(1-3):67-72. doi: 10.1016/0014-2999(96)00206-3.
Administration of the neuropeptide, arginine vasopressin, can reduce the rate of dissipation of functional ethanol tolerance in mice that have acquired that tolerance. We previously showed that intracerebroventricular vasopressin administration can also produce an increase in septal c-fos mRNA levels. To evaluate the role of the increased expression of c-fos in the ability of vasopressin to maintain tolerance, ethanol-tolerant mice were given intracerebroventricular injections of vasopressin in the presence or absence of an antisense oligonucleotide to c-fos. The antisense oligonucleotide completely blocked the ability of vasopressin to maintain ethanol tolerance, while a missense oligonucleotide was without effect. The antisense oligonucleotide also attenuated the increase in septal c-fos mRNA levels caused by vasopressin. The results provide evidence for a role of c-fos expression in the maintenance of ethanol tolerance by vasopressin.
给予神经肽精氨酸加压素,可降低已获得功能性乙醇耐受性的小鼠体内乙醇耐受性的消散速率。我们之前表明,脑室内注射加压素也可使隔区c-fos信使核糖核酸水平升高。为了评估c-fos表达增加在加压素维持耐受性能力中的作用,在有或没有针对c-fos的反义寡核苷酸的情况下,给乙醇耐受小鼠脑室内注射加压素。反义寡核苷酸完全阻断了加压素维持乙醇耐受性的能力,而错义寡核苷酸则没有效果。反义寡核苷酸也减弱了加压素引起的隔区c-fos信使核糖核酸水平的升高。这些结果为c-fos表达在加压素维持乙醇耐受性中的作用提供了证据。